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[[Lyme disease]]'s neurologic syndrome, called Lyme encephalopathy, is associated with subtle memory and cognitive difficulties, among other issues.<ref name=MayoClin2008>{{cite journal |last1=Bratton |first1=Robert L. |last2=Whiteside |first2=John W. |last3=Hovan |first3=Michael J. |last4=Engle |first4=Richard L. |last5=Edwards |first5=Frederick D. |title=Diagnosis and Treatment of Lyme Disease |journal=Mayo Clinic Proceedings |date=May 2008 |volume=83 |issue=5 |pages=566–571 |doi=10.4065/83.5.566 |pmid=18452688 |doi-access=free }}</ref> Lyme can cause a chronic [[encephalomyelitis]] that resembles [[multiple sclerosis]]. It may be progressive and can involve cognitive impairment, [https://www.botanicalremediesllc.com/blog/top-helpful-tips-to-improve-your-mental-focus/ brain fog], [[migraine]]s, balance issues, and extensive other issues.{{citation needed|date=June 2022}}
[[Lyme disease]]'s neurologic syndrome, called Lyme encephalopathy, is associated with subtle memory and cognitive difficulties, among other issues.<ref name=MayoClin2008>{{cite journal |last1=Bratton |first1=Robert L. |last2=Whiteside |first2=John W. |last3=Hovan |first3=Michael J. |last4=Engle |first4=Richard L. |last5=Edwards |first5=Frederick D. |title=Diagnosis and Treatment of Lyme Disease |journal=Mayo Clinic Proceedings |date=May 2008 |volume=83 |issue=5 |pages=566–571 |doi=10.4065/83.5.566 |pmid=18452688 |doi-access=free }}</ref> Lyme can cause a chronic [[encephalomyelitis]] that resembles [[multiple sclerosis]]. It may be progressive and can involve cognitive impairment, [https://www.botanicalremediesllc.com/blog/top-helpful-tips-to-improve-your-mental-focus/ brain fog], [[migraine]]s, balance issues, and extensive other issues.{{citation needed|date=June 2022}}

Brain fog and other neurological symptoms may also result from [[mold]] exposure.<ref name="pmid19854819">{{cite journal | vauthors = Empting LD | title = Neurologic and neuropsychiatric syndrome features of mold and mycotoxin exposure | journal = Toxicol Ind Health | volume = 25 | issue = 9-10 | pages = 577–81 | date = 2009 | pmid = 19854819 | doi = 10.1177/0748233709348393 | url = }}</ref><ref name="pmid28848553">{{cite journal | vauthors = Valtonen V | title = Clinical Diagnosis of the Dampness and Mold Hypersensitivity Syndrome: Review of the Literature and Suggested Diagnostic Criteria | journal = Front Immunol | volume = 8 | issue = | pages = 951 | date = 2017 | pmid = 28848553 | pmc = 5554125 | doi = 10.3389/fimmu.2017.00951 | url = }}</ref><ref name="pmid36638914">{{cite journal | vauthors = Harding CF, Liao D, Persaud R, DeStefano RA, Page KG, Stalbow LL, Roa T, Ford JC, Goman KD, Pytte CL | title = Differential effects of exposure to toxic or nontoxic mold spores on brain inflammation and Morris water maze performance | journal = Behav Brain Res | volume = 442 | issue = | pages = 114294 | date = March 2023 | pmid = 36638914 | doi = 10.1016/j.bbr.2023.114294 | url = }}</ref><ref name="pmid29880330">{{cite journal | vauthors = Ratnaseelan AM, Tsilioni I, Theoharides TC | title = Effects of Mycotoxins on Neuropsychiatric Symptoms and Immune Processes | journal = Clin Ther | volume = 40 | issue = 6 | pages = 903–917 | date = June 2018 | pmid = 29880330 | doi = 10.1016/j.clinthera.2018.05.004 | url = }}</ref><ref name="pmid31751617">{{cite journal | vauthors = Harding CF, Pytte CL, Page KG, Ryberg KJ, Normand E, Remigio GJ, DeStefano RA, Morris DB, Voronina J, Lopez A, Stalbow LA, Williams EP, Abreu N | title = Mold inhalation causes innate immune activation, neural, cognitive and emotional dysfunction | journal = Brain Behav Immun | volume = 87 | issue = | pages = 218–228 | date = July 2020 | pmid = 31751617 | pmc = 7231651 | doi = 10.1016/j.bbi.2019.11.006 | url = }}</ref> This may be due to [[mycotoxin]] exposure and consequent innate [[immune system]] activation and [[inflammation]], including in the central nervous system.<ref name="pmid19854819" /><ref name="pmid28848553" /><ref name="pmid36638914" /><ref name="pmid29880330" /><ref name="pmid31751617" /> However, adverse neurological health effects of mold exposure are controversial due to inadequate research and data, and more research is needed in this area.<ref name="pmid28453304">{{cite journal | vauthors = Rudert A, Portnoy J | title = Mold allergy: is it real and what do we do about it? | journal = Expert Rev Clin Immunol | volume = 13 | issue = 8 | pages = 823–835 | date = August 2017 | pmid = 28453304 | doi = 10.1080/1744666X.2017.1324298 | url = }}</ref><ref name="pmid28299723">{{cite journal | vauthors = Borchers AT, Chang C, Eric Gershwin M | title = Mold and Human Health: a Reality Check | journal = Clin Rev Allergy Immunol | volume = 52 | issue = 3 | pages = 305–322 | date = June 2017 | pmid = 28299723 | doi = 10.1007/s12016-017-8601-z | url = }}</ref><ref name="pmid19854819" /><ref name="pmid36638914" /><ref name="pmid31751617" />


==See also==
==See also==

Revision as of 18:19, 12 May 2023

Clouding of consciousness (also known as brain fog or mental fog)[1][2] occurs when a person is slightly less wakeful or aware than normal.[3] They are not as aware of time or their surroundings and find it difficult to pay attention.[3] People describe this subjective sensation as their mind being "foggy".[4]

Background

The term clouding of consciousness has always denoted the main pathogenetic feature of delirium since physician Georg Greiner[5] pioneered the term (Verdunkelung des Bewusstseins) in 1817.[6] The Diagnostic and Statistical Manual of Mental Disorders (DSM) has historically used the term in its definition of delirium.[7] However, the DSM-III-R and the DSM-IV replaced "clouding of consciousness" with "disturbance of consciousness" to make it easier to operationalize, but it is still fundamentally the same thing.[8] Clouding of consciousness may be less severe than delirium on a spectrum of abnormal consciousness.[3][9][10] Clouding of consciousness may be synonymous with subsyndromal delirium.[11]

Subsyndromal delirium differs from normal delirium by being overall less severe, lacking acuteness in onset and duration, having a relatively stable sleep-wake cycle, and having relatively stable motor alterations.[12] The significant clinical features of subsyndromal delirium are inattention, thought process abnormalities, comprehension abnormalities, and language abnormalities.[12] The full clinical manifestations of delirium may never be reached.[11] Among intensive care unit patients, subsyndromal subjects were as likely to survive as patients with a Delirium Screening Checklist score of 0, but required extended care at rates greater than 0-scoring patients (although lower rates than those with full delirium)[11] or have a decreased post-discharge level of functional independence vs. the general population but still more independence than full delirium.[12]

In clinical practice, there is no standard test that is exclusive and specific; therefore, the diagnosis depends on the subjective impression of the physician. The DSM-IV-TR instructs clinicians to code subsyndromal delirium presentations under the miscellaneous category of "cognitive disorder not otherwise specified".[13]

Psychopathology

The conceptual model of clouding of consciousness is that of a part of the brain regulating the "overall level" of the consciousness part of the brain, which is responsible for awareness of oneself and of the environment.[3][14] Various etiologies disturb this regulating part of the brain, which in turn disturbs the "overall level" of consciousness.[15] This system of a sort of general activation of consciousness is referred to as "arousal" or "wakefulness".[14]

It is not necessarily accompanied by drowsiness, however.[16] Patients may be awake (not sleepy) yet still have a clouded consciousness (disorder of wakefulness).[17] Paradoxically, affected individuals say that they are "awake but, in another way, not".[18] Lipowski points out that decreased "wakefulness" as used here is not exactly synonymous with drowsiness. One is a stage on the way to coma, the other on the way to sleep which is very different.[19][20]

The affected person experiences a subjective sensation of mental clouding described in the patient's own words as feeling "foggy".[4] One patient described it as "I thought it became like misty, in some way... the outlines were sort of fuzzy".[18] Others may describe a "spaced out" feeling.[21] Affected individuals compare their overall experience to that of a dream because as in a dream consciousness, attention, orientation to time and place, perceptions, and awareness are disturbed.[22] Barbara Schildkrout, MD, a board-certified psychiatrist and clinical instructor in psychiatry at the Harvard Medical School described her subjective experience of clouding of consciousness, or what she also called "mental fog", after taking a single dose of chlorpheniramine an antihistamine for her allergy to cottonwood while on a cross-country road trip. She described feeling "out of it" and being in a "dreamy state". She described a sense of not trusting her own judgment and a dulled awareness, not knowing how long time went by.[1] Clouding of consciousness is not the same thing as depersonalization even though people affected by both compare their experience to that of a dream. Psychometric tests produce little evidence of a relationship between clouding of consciousness and depersonalization.[23]

This may affect performance on virtually any cognitive task.[1] As one author put it, "It should be apparent that cognition is not possible without a reasonable degree of arousal."[3] Cognition includes perception, memory, learning, executive functions, language, constructive abilities, voluntary motor control, attention, and mental speed. The most significant, however, are inattention, thought process abnormalities, comprehension abnormalities, and language abnormalities.[12] The extent of the impairment is variable because inattention may impair several cognitive functions. Affected individuals may complain of forgetfulness, being "confused",[24] or being "unable to think straight".[24] Despite the similarities, subsyndromal delirium is not the same thing as mild cognitive impairment; the fundamental difference is that mild cognitive impairment is a dementia-like impairment, which does not involve a disturbance in arousal (wakefulness).[25]

In diseases

The emerging concept of sluggish cognitive tempo has also been implicated in the expression of 'brain fog' symptoms.[26]

Patients recovering from COVID-19 report experiencing 'brain fog', which can reflect a wide variety of neurological and psychological symptoms linked to COVID-19.[27]

Many people with fibromyalgia experience cognitive problems[28] (known as "fibrofog" or "brainfog"), which may involved impaired concentration,[29][30][unreliable medical source?][31] problems with short[32]- and long-term memory, short-term memory consolidation,[32] working memory,[33] impaired speed of performance,[32] inability to multi-task, cognitive overload,[32] and diminished attention span. About 75% of fibromyalgia patients report significant problems with concentration, memory, and multitasking.[34] A 2018 meta-analysis found that the largest differences between fibromyalgia patients and healthy subjects were for inhibitory control, memory, and processing speed.[34] Many of these are also common symptoms of ADHD (attention deficit hyperactivity disorder), and the two conditions have been linked via studies, to the point that a diagnosis of fibromyalgia has been proposed as an indication to also screen for ADHD.[35][36][37] In particular, the "brain fog" of ADHD has been linked to "fibro fog".[38] It is alternatively hypothesized that the increased pain compromises attention systems, resulting in cognitive problems.[34]

In chronic fatigue syndrome, also known as myalgic encephalomyelitis, the CDC's recommended criteria for diagnosis[39] include that one of the following symptoms must be present:[39]

  • Problems with thinking and memory (cognitive dysfunction, sometimes described as "brain fog")
  • While standing or sitting upright; lightheadedness, dizziness, weakness, fainting or vision changes may occur (orthostatic intolerance)

Lyme disease's neurologic syndrome, called Lyme encephalopathy, is associated with subtle memory and cognitive difficulties, among other issues.[40] Lyme can cause a chronic encephalomyelitis that resembles multiple sclerosis. It may be progressive and can involve cognitive impairment, brain fog, migraines, balance issues, and extensive other issues.[citation needed]

Brain fog and other neurological symptoms may also result from mold exposure.[41][42][43][44][45] This may be due to mycotoxin exposure and consequent innate immune system activation and inflammation, including in the central nervous system.[41][42][43][44][45] However, adverse neurological health effects of mold exposure are controversial due to inadequate research and data, and more research is needed in this area.[46][47][41][43][45]

See also

References

  1. ^ a b c Barbara Schildkrout (2011). Unmasking Psychological Symptoms. John Wiley & Sons. pp. 183–184. ISBN 9780470639078.
  2. ^ M. Basavanna (2000). Dictionary of psychology. Allied Publishers. p. 65. ISBN 8177640305.
  3. ^ a b c d e Plum and Posner's diagnosis of stupor and coma. Oxford University Press. 2007. pp. 5–6. ISBN 9780199886531.
  4. ^ a b Augusto Caraceni; Luigi Grassi (2011). Delirium: Acute Confusional States in Palliative Medicine. Oxford University Press. p. 82. ISBN 9780199572052.
  5. ^ Georg Friedrich Christoph Greiner (1817). Der Traum und das fieberhafte Irreseyn: ein physiologisch-psychologischer Versuch. F. A Brockhaus. OCLC 695736431.
  6. ^ Augusto Caraceni; Luigi Grassi (2011). Delirium: Acute Confusional States in Palliative Medicine. Oxford University Press. p. 2. ISBN 9780199572052.
  7. ^ George Stein; Greg Wilkinson (April 2007). Seminars in General Adult Psychiatry. RCPsych Publications. p. 490. ISBN 978-1904671442.
  8. ^ Dan G. Blazer; Adrienne O. van Nieuwenhuizen (2012). "Evidence for the Diagnostic Criteria of Delirium". Curr Opin Psychiatry. 25 (3): 239–243. doi:10.1097/yco.0b013e3283523ce8. PMID 22449764. S2CID 39516431.
  9. ^ Anthony David; Simon Fleminger; Michael Kopelman; Simon Lovestone; John Mellers (April 2012). Lishman's Organic Psychiatry: A Textbook of Neuropsychiatry. John Wiley & Sons. p. 5. ISBN 9780470675076.
  10. ^ Fang Gao Smith (April 2010). Core Topics in Critical Care Medicine. Cambridge University Press. p. 312. ISBN 978-1139489683.
  11. ^ a b c Sébastien Ouimet; Riker, R; Bergeron, N; Cossette, M; Kavanagh, B; Skrobik, Y; et al. (2007). "Subsyndromal delirium in the ICU: evidence for a disease spectrum". Intensive Care Med. 33 (6): 1007–1013. doi:10.1007/s00134-007-0618-y. PMID 17404704. S2CID 20565946.
  12. ^ a b c d David Meagher; Adamis, D.; Trzepacz, P.; Leonard, M.; et al. (2012). "Features of subsyndromal and persistent delirium". The British Journal of Psychiatry. 200 (1): 37–44. doi:10.1192/bjp.bp.111.095273. PMID 22075650.
  13. ^ Augusto Caraceni; Luigi Grassi (2011). Delirium: Acute Confusional States in Palliative Medicine. Oxford University Press. p. 11. ISBN 9780199572052.
  14. ^ a b Augusto Caraceni; Luigi Grassi (2011). Delirium: Acute Confusional States in Palliative Medicine. Oxford University Press. pp. 19–21. ISBN 9780199572052.
  15. ^ Yudofsky & Hales (2008). The American Psychiatric Publishing textbook of neuropsychiatry and behavioral neurosciences. American Psychiatric Pub. p. 477. ISBN 978-1585622399.
  16. ^ Roger A. MacKinnon; Robert Michels; Peter J. Buckley (2006). The Psychiatric Interview in Clinical Practice 2nd edition. American Psychiatric Publishing, Inc. pp. 462–464.
  17. ^ Plum and Posner's diagnosis of stupor and coma. Oxford University Press. 2007. p. 8. ISBN 9780198043362.
  18. ^ a b G Sorensen Duppils; K Wikblad (May 2007). "Patients' experiences of being delirious". Journal of Clinical Nursing. 16 (5): 810–818. doi:10.1111/j.1365-2702.2006.01806.x. PMID 17462032.
  19. ^ Lipowski ZJ. (1967). "Delirium, clouding of consciousness and confusion". Journal of Nervous and Mental Disease. 145 (3): 227–255. doi:10.1097/00005053-196709000-00006. PMID 4863989.
  20. ^ William Alwyn Lishman (1998). Organic Psychiatry: The Psychological Consequences of Cerebral Disorder. John Wiley & Sons. p. 4.
  21. ^ Fred Ovsiew, M.D. (1999). Neuropsychiatry and Mental Health Services. American Psychiatric Press, Inc. p. 170. ISBN 0880487305.
  22. ^ Simon Fleminger (2002). "Remembering delirium". The British Journal of Psychiatry. 180 (1): 4–5. doi:10.1192/bjp.180.1.4. PMID 11772842.
  23. ^ Sedman, G. (July 1970). "Theories of Depersonalization: A Re-appraisal". British Journal of Psychiatry. 117 (536): 1–14. doi:10.1192/s0007125000192104. PMID 4920886. S2CID 246610704.
  24. ^ a b John Noble; Harry L. Greene (1996). Textbook of Primary Care Medicine. Mosby. p. 1325.
  25. ^ Plum and Posner's diagnosis of stupor and coma. Oxford University Press. 2007. p. 7. ISBN 9780199886531.
  26. ^ Barkley, Russell A. (2013). Taking Charge of ADHD: The Complete, Authoritative Guide for Parents. Guilford Publications. p. 150. ISBN 978-1-4625-0789-4.
  27. ^ Koralnik, Igor J.; Tyler, Kenneth L. (July 2020). "COVID ‐19: A Global Threat to the Nervous System". Annals of Neurology. 88 (1): 1–11. doi:10.1002/ana.25807. PMC 7300753. PMID 32506549.
  28. ^ Glass, Jennifer M. (November 2006). "Cognitive dysfunction in fibromyalgia and chronic fatigue syndrome: New trends and future directions". Current Rheumatology Reports. 8 (6): 425–429. doi:10.1007/s11926-006-0036-0. PMID 17092441. S2CID 27103590.
  29. ^ Arnold, Lesley M.; Bennett, Robert M.; Crofford, Leslie J.; Dean, Linda E.; Clauw, Daniel J.; Goldenberg, Don L.; Fitzcharles, Mary-Ann; Paiva, Eduardo S.; Staud, Roland; Sarzi-Puttini, Piercarlo; Buskila, Dan; Macfarlane, Gary J. (June 2019). "AAPT Diagnostic Criteria for Fibromyalgia". The Journal of Pain. 20 (6): 611–628. doi:10.1016/j.jpain.2018.10.008. PMID 30453109. S2CID 53872511.
  30. ^ Williams, David A; Clauw, Daniel J; Glass, Jennifer M (April 2011). "Perceived Cognitive Dysfunction in Fibromyalgia Syndrome". Journal of Musculoskeletal Pain. 19 (2): 66–75. doi:10.3109/10582452.2011.558989. S2CID 144893303.
  31. ^ [unreliable medical source?] Leavitt, Frank; Katz, Robert S.; Mills, Megan; Heard, Amy R. (April 2002). "Cognitive and Dissociative Manifestations in Fibromyalgia". JCR: Journal of Clinical Rheumatology. 8 (2): 77–84. doi:10.1097/00124743-200204000-00003. PMID 17041327. S2CID 12352666.
  32. ^ a b c d Buskila, Dan; Cohen, Hagit (October 2007). "Comorbidity of fibromyalgia and psychiatric disorders". Current Pain and Headache Reports. 11 (5): 333–338. doi:10.1007/s11916-007-0214-4. PMID 17894922. S2CID 28038437.
  33. ^ Mercado, Francisco; Ferrera, David; Fernandes-Magalhaes, Roberto; Peláez, Irene; Barjola, Paloma (2 March 2022). "Altered Subprocesses of Working Memory in Patients with Fibromyalgia: An Event-Related Potential Study Using N -Back Task". Pain Medicine. 23 (3): 475–487. doi:10.1093/pm/pnab190. PMID 34145889.
  34. ^ a b c Bell, Tyler; Trost, Zina; Buelow, Melissa T.; Clay, Olivio; Younger, Jarred; Moore, David; Crowe, Michael (9 August 2018). "Meta-analysis of cognitive performance in fibromyalgia". Journal of Clinical and Experimental Neuropsychology. 40 (7): 698–714. doi:10.1080/13803395.2017.1422699. PMC 6151134. PMID 29388512.
  35. ^ Bou Khalil, Rami; Khoury, Elie; Richa, Sami (1 September 2018). "The Comorbidity of Fibromyalgia Syndrome and Attention Deficit and Hyperactivity Disorder from a Pathogenic Perspective". Pain Medicine. 19 (9): 1705–1709. doi:10.1093/pm/pny142. PMID 30053155.
  36. ^ Yilmaz, Ertan; Tamam, Lut (24 July 2018). "Attention-deficit hyperactivity disorder and impulsivity in female patients with fibromyalgia". Neuropsychiatric Disease and Treatment. 14: 1883–1889. doi:10.2147/NDT.S159312. PMC 6063452. PMID 30100723.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  37. ^ "Study Suggests Screening Patients with Fibromyalgia Syndrome for ADHD".
  38. ^ "Connection between Fibromyalgia and ADHD".
  39. ^ a b "Symptoms of ME/CFS | Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)". CDC. 9 February 2021.
  40. ^ Bratton, Robert L.; Whiteside, John W.; Hovan, Michael J.; Engle, Richard L.; Edwards, Frederick D. (May 2008). "Diagnosis and Treatment of Lyme Disease". Mayo Clinic Proceedings. 83 (5): 566–571. doi:10.4065/83.5.566. PMID 18452688.
  41. ^ a b c Empting LD (2009). "Neurologic and neuropsychiatric syndrome features of mold and mycotoxin exposure". Toxicol Ind Health. 25 (9–10): 577–81. doi:10.1177/0748233709348393. PMID 19854819.
  42. ^ a b Valtonen V (2017). "Clinical Diagnosis of the Dampness and Mold Hypersensitivity Syndrome: Review of the Literature and Suggested Diagnostic Criteria". Front Immunol. 8: 951. doi:10.3389/fimmu.2017.00951. PMC 5554125. PMID 28848553.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  43. ^ a b c Harding CF, Liao D, Persaud R, DeStefano RA, Page KG, Stalbow LL, Roa T, Ford JC, Goman KD, Pytte CL (March 2023). "Differential effects of exposure to toxic or nontoxic mold spores on brain inflammation and Morris water maze performance". Behav Brain Res. 442: 114294. doi:10.1016/j.bbr.2023.114294. PMID 36638914.
  44. ^ a b Ratnaseelan AM, Tsilioni I, Theoharides TC (June 2018). "Effects of Mycotoxins on Neuropsychiatric Symptoms and Immune Processes". Clin Ther. 40 (6): 903–917. doi:10.1016/j.clinthera.2018.05.004. PMID 29880330.
  45. ^ a b c Harding CF, Pytte CL, Page KG, Ryberg KJ, Normand E, Remigio GJ, DeStefano RA, Morris DB, Voronina J, Lopez A, Stalbow LA, Williams EP, Abreu N (July 2020). "Mold inhalation causes innate immune activation, neural, cognitive and emotional dysfunction". Brain Behav Immun. 87: 218–228. doi:10.1016/j.bbi.2019.11.006. PMC 7231651. PMID 31751617.
  46. ^ Rudert A, Portnoy J (August 2017). "Mold allergy: is it real and what do we do about it?". Expert Rev Clin Immunol. 13 (8): 823–835. doi:10.1080/1744666X.2017.1324298. PMID 28453304.
  47. ^ Borchers AT, Chang C, Eric Gershwin M (June 2017). "Mold and Human Health: a Reality Check". Clin Rev Allergy Immunol. 52 (3): 305–322. doi:10.1007/s12016-017-8601-z. PMID 28299723.